Dentinogenesis imperfecta type II: a case report
Bruno Carvalho Albeny Morais+4 more
openalex +2 more sources
Treatment of anterior open bite in a patient with dentinogenesis imperfecta [PDF]
Takayuki Tsujimoto+2 more
openalex +1 more source
Study of enamel and dentin in primary teeth with dentinogenesis imperfecta type I: A case report [PDF]
Yoko Kamasaki+4 more
openalex +1 more source
Dentin Sialophosphoprotein Knockout Mouse Teeth Display Widened Predentin Zone and Develop Defective Dentin Mineralization Similar to Human Dentinogenesis Imperfecta Type III [PDF]
Taduru Sreenath+9 more
openalex +3 more sources
Dentinogenesis imperfecta type II: approach for dental treatment
INTRODUCTION: Dentinogenesis imperfecta (DI) is a hereditary dentin development disorder that affects both primary and permanent dentitions. The DI characteristics are discolored and translucent teeth ranging from gray to brownish-blue or amber.
Raquel Mantuaneli Scarel-Caminaga+5 more
doaj
An Aesthetic and Economic Approach of Smile Designing for a Patient With Dentinogenesis Imperfecta: A Rare Case Entity. [PDF]
Kumar A+4 more
europepmc +1 more source
Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience. [PDF]
Monteiro J+6 more
europepmc +1 more source
A novel approach to full-mouth rehabilitation of dentinogenesis imperfecta type II: Case series with review of literature. [PDF]
Zhang Y+7 more
europepmc +1 more source
Dentinogenesis imperfecta type II in Swedish children and adolescents. [PDF]
Andersson K+3 more
europepmc +1 more source
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlation. [PDF]
Chetty M+3 more
europepmc +1 more source